(S)-tert-Butyl 6-amino-2-((tert-butoxycarbonyl)amino)hexanoate hydrochloride

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Reagent Code: #38588
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CAS Number 7750-45-0

science Other reagents with same CAS 7750-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.87 g/mol
Formula C₁₅H₃₁ClN₂O₄
badge Registry Numbers
MDL Number MFCD08275791
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a key intermediate in the production of biologically active molecules. Its structure, featuring both amino and tert-butoxycarbonyl (Boc) protecting groups, makes it valuable in organic synthesis, particularly in peptide coupling reactions where selective protection and deprotection are required. It is often employed in the development of pharmaceutical compounds, including drugs targeting neurological disorders and enzyme inhibitors. Additionally, its hydrochloride form enhances stability and solubility, facilitating its use in various chemical processes. The compound is also relevant in research focused on amino acid modification and the exploration of novel therapeutic agents.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,083.00
inventory 250mg
10-20 days ฿3,537.00

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(S)-tert-Butyl 6-amino-2-((tert-butoxycarbonyl)amino)hexanoate hydrochloride
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This compound is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a key intermediate in the production of biologically active molecules. Its structure, featuring both amino and tert-butoxycarbonyl (Boc) protecting groups, makes it valuable in organic synthesis, particularly in peptide coupling reactions where selective protection and deprotection are required. It is often employed in the development of pharmaceutical compounds, including drugs targeting neurological

This compound is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a key intermediate in the production of biologically active molecules. Its structure, featuring both amino and tert-butoxycarbonyl (Boc) protecting groups, makes it valuable in organic synthesis, particularly in peptide coupling reactions where selective protection and deprotection are required. It is often employed in the development of pharmaceutical compounds, including drugs targeting neurological disorders and enzyme inhibitors. Additionally, its hydrochloride form enhances stability and solubility, facilitating its use in various chemical processes. The compound is also relevant in research focused on amino acid modification and the exploration of novel therapeutic agents.

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